Foot Saver

Product NDC
50017-020
Requested package NDC
50017-020-01
11-digit product format
500170020
Labeler code
50017
Product ID
50017-020_e10777b2-6fe0-b94b-e053-2a95a90a77a8
Type
HUMAN OTC DRUG
Nonproprietary name
Antiperspirant
Dosage form
GEL
Route
TOPICAL
Labeler
Neat Feat Products Limited
Application
part350
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2022-04-05
Marketing end
0000-00-00
Substance
ALUMINUM CHLOROHYDRATE
Active strength
14 g/60mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage50017-02050017-020-01IInactivated by FDA2026-08-11

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 9 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05IInactivated by FDAd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26IInactivated by FDAf5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31IInactivated by FDA2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28IInactivated by FDAa1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21IInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10IInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31UExcluded because listing certification expired302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20UExcluded because listing certification expireded331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10UExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50017-020-012025-01-30C16284748780-12cef2736-59c3-d83d-e063-dadaa90ab31fNEAT® 3B FOOT SAVER ROLL-ON

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50017-020-01Foot Saver1 in 1 BOXGEL112
50017-020-02Foot Saver60 mL in 1 TUBE, WITH APPLICATORGEL6012

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50017-020FOOT SAVER (ANTIPERSPIRANT) GEL [NEAT FEAT PRODUCTS LIMITED]12Legacy NDC, 2 package rows20231102_7e41f204-277a-4ed6-b6fc-b50ceb6e6ccd.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50017-020-01500170020011 TUBE, WITH APPLICATOR in 1 BOX (50017-020-01) > 60 mL in 1 TUBE, WITH APPLICATOR (50017-020-02) 2022-04-050000-00-00NoNoCurrent